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Perturbation of genomic imprinting in oligozoospermia

Pages 27-30 | Received 29 Oct 2008, Accepted 03 Nov 2008, Published online: 01 Jan 2009

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Nervana Bayoumy, Mohamed El-Shabrawi & Hesham Nada. (2020) Association of ICAM-1 gene variant rs5498 (1462A>G) with non-obstructive azoospermia. Human Fertility 23:4, pages 234-238.
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Ying Chan, Hongguo Jiang, Lan Ma, Jinbao Chen, Dongya Li, Yushi Meng, Ying Luo & Wenru Tang. (2015) No association of TP53 codon 72 SNP with male infertility: a study in a Chinese population and a meta-analysis. Systems Biology in Reproductive Medicine 61:4, pages 222-227.
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John C Rotondo, Rita Selvatici, Maura Di Domenico, Roberto Marci, Fortunato Vesce, Mauro Tognon & Fernanda Martini. (2013) Methylation loss at H19 imprinted gene correlates with gene promoter hypermethylation in semen samples from infertile males. Epigenetics 8:9, pages 990-997.
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Kenneth I. Aston & Douglas T. Carrell. (2012) Emerging evidence for the role of genomic instability in male factor infertility. Systems Biology in Reproductive Medicine 58:2, pages 71-80.
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Douglas T. Carrell & Kenneth I. Aston. (2011) The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility. Systems Biology in Reproductive Medicine 57:1-2, pages 17-26.
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